iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs3656054	snp	A/C	0.5	0	intron-variant	Rnf10	Mm_Celera	5:115264973	TATATGACACATACA[A/C]ACACACACACACACA	50849
rs4138145	snp	C/T	0.5	0	intron-variant	Rnf10	Mm_Celera	5:115264969	TATATATATGACACA[C/T]ACAAACACACACACA	50849
rs6261339	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Rnf10	Mm_Celera	5:115261519	caggagccgggagcc[A/G]gngcattagagtaac	50849
rs6261341	snp	A/C	0.5	0	intron-variant, upstream-variant-2KB	Rnf10	Mm_Celera	5:115261521	ggagccgggagccng[A/C]gcattagagtaacca	50849
rs6261804	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Rnf10	Mm_Celera	5:115261586	TACCTCAATCCACAA[A/G]TAAATAATATATAAA	50849
rs6261869	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Rnf10	Mm_Celera	5:115261624	CTGTCTCAAATAAAG[C/T]TGAAGTctaaagagg	50849
rs6275520	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Rnf10	Mm_Celera	5:115261811	ataaatgcaggcaaa[C/T]acacacataaaataa	50849
rs6328077	snp	C/T	0.5	0	intron-variant	Rnf10	Mm_Celera	5:115271215	ggccagcctggtcta[C/T]agagtgagttncagg	50849
rs6328094	snp	C/T	0.5	0	intron-variant	Rnf10	Mm_Celera	5:115271226	tctanagagtgagtt[C/T]caggacaggcaagga	50849
rs6328576	snp	C/T	0.5	0	intron-variant	Rnf10	Mm_Celera	5:115271276	cgaaaaaccaaaAGA[C/T]TGATTGAAAAAAAAA	50849
rs6343708	snp	A/C	0.5	0	intron-variant	Rnf10	Mm_Celera	5:115271774	CTGAACCTAAATGAA[A/C]TGAATGCAGGGTCTG	50849
rs13474671	snp	A/G			utr-variant-3-prime	Rnf10	Mm_Celera	5:115241880	AAAGCCCCTCCCCCC[A/G]CCCCAAGCTAATCAA	50849
rs13474673	snp	C/T			missense	Rnf10	Mm_Celera	5:115257004	AGTGGGGACACAAGC[C/T]TTTCAACAAGGAGCT	50849
rs13474674	snp	C/T			utr-variant-3-prime	Rnf10	Mm_Celera	5:115241899	GTATTTGAGTTTGAA[C/T]AGATTGATTAGCTTG	50849
rs13474675	snp	G/T			synonymous-codon	Rnf10	GRCm38.p3	5:115249147	GGAGTATCTGTCTGC[G/T]TTTGATGATGAAGCT	50849
rs13474676	snp	A/G			stop-gained	Rnf10	Mm_Celera	5:115250111	GCAGCTCAGCCAGTA[A/G]TCCAAGCTGCTGCTG	50849
rs13474677	snp	C/G			synonymous-codon	Rnf10	Mm_Celera	5:115251109	GTTGGTGGCCCTGCC[C/G]AAATCCAAGTGGGTG	50849
rs13474678	snp	C/T	0.32	0.24	synonymous-codon	Rnf10	Mm_Celera	5:115249003	TCTGGGAGAGGGGAC[C/T]GTTGGTCCTGAGATG	50849
rs13474679	snp	A/G			missense	Rnf10	Mm_Celera	5:115242499	TGATGGGGAGAGTGA[A/G]AATTCTGACCGTGTT	50849
rs13474680	snp	A/G			missense	Rnf10	Mm_Celera	5:115242514	CGCCCCTGTGGACAG[A/G]GATGGGGAGAGTGAC	50849
rs13474681	snp	C/G/T			synonymous-codon	Rnf10	Mm_Celera	5:115249487	AGGAGTGGCTGGAGG[C/G/T]GGAGGGGAGGTCACT	50849
rs29530915	snp	A/G	0.444444	0.157135	upstream-variant-2KB	Rnf10	Mm_Celera	5:115273133	GAACTCTTTGTGTGC[A/G]ACAGTCTGGCTTCCA	50849
rs29566887	snp	A/G	0.375	0.216506	intron-variant	Rnf10	Mm_Celera	5:115268820	CCAAGGCTGTAGACT[A/G]AAAGATCAAGAAACT	50849
rs29583537	snp	A/G	0.375	0.216506	intron-variant	Rnf10	Mm_Celera	5:115250255	CTGGGCTAGCTCAAA[A/G]ACCTAAGCAGCCAGA	50849
rs29633811	snp	C/T	0.444444	0.157135	intron-variant	Rnf10	Mm_Celera	5:115250703	TGCCTGCCCCAGGAC[C/T]TTAGTCTTTAAGACA	50849
rs29680275	snp	C/T	0.375	0.216506	upstream-variant-2KB	Rnf10	Mm_Celera	5:115273817	TGAGTGGAATTTTAG[C/T]AATCGTGTATGTAGG	50849
rs29766342	snp	A/G	0.375	0.216506	intron-variant	Rnf10	Mm_Celera	5:115242115	CACAGTACTGTGGGC[A/G]CCCAGGTGAAATGGC	50849
rs29779958	snp	A/C	0.32	0.24	intron-variant	Rnf10	Mm_Celera	5:115270859	GGCACTGGAAAACTA[A/C]GGGGTGTGCTCTTCC	50849
rs29824774	snp	C/G	0.444444	0.157135	intron-variant	Rnf10	Mm_Celera	5:115258391	CCGTCTGTCCGCTGG[C/G]CTGCTCCAGGTCAGC	50849
rs32137514	snp	A/G			intron-variant	Rnf10	Mm_Celera	5:115256825	CCACTCCTGGTCCCA[A/G]AAGTCACGGCAAGCA	50849
rs32137515	snp	G/T			intron-variant	Rnf10	Mm_Celera	5:115256920	CCCCCTGACTGGTTA[G/T]ATGAGGTGTCCTCCT	50849
rs32137516	snp	C/T			intron-variant	Rnf10	Mm_Celera	5:115257335	GCATCCCGACTGTCC[C/T]GTCGCCCTGCTCAGC	50849
rs32137517	snp	A/G	0.375	0.216506	intron-variant	Rnf10	Mm_Celera	5:115257336	CATCCCGACTGTCCC[A/G]TCGCCCTGCTCAGCA	50849
rs32137518	snp	C/T			intron-variant	Rnf10	Mm_Celera	5:115257512	CAAACCTTTTACCTC[C/T]ATGTCAAATCCACAC	50849
rs32137519	snp	C/T			intron-variant	Rnf10	Mm_Celera	5:115258182	GATGGAGTTAGAGCA[C/T]GAAGGTAAGAACTAG	50849
rs32137520	snp	A/G			intron-variant	Rnf10	Mm_Celera	5:115258378	AACGTCCGTCTGTCC[A/G]TCTGTCCGCTGGGCT	50849
rs32137521	snp	C/T			intron-variant	Rnf10	Mm_Celera	5:115258387	CTGTCCGTCTGTCCG[C/T]TGGGCTGCTCCAGGT	50849
rs32137522	snp	G/T			intron-variant	Rnf10	Mm_Celera	5:115258904	TTTAATGCCATTATT[G/T]ACTTTAATGTGCAAG	50849
rs32137523	snp	A/T			intron-variant	Rnf10	Mm_Celera	5:115259689	ACACACAGCATGGAC[A/T]GTCAAACAACAGCAC	50849
rs32138394	snp	A/G			intron-variant, upstream-variant-2KB	Rnf10	Mm_Celera	5:115260344	AAATAAAAGTAATAA[A/G]TTTAATGTTTTCCCA	50849
rs32138395	snp	A/G			intron-variant, upstream-variant-2KB	Rnf10	Mm_Celera	5:115260445	CTGTGAGAAAGCTAA[A/G]CTTAGTCCATAGCAC	50849
rs32138396	snp	A/T			intron-variant, upstream-variant-2KB	Rnf10	Mm_Celera	5:115260766	CACGCTATGGAAGCT[A/T]CAGAGTTAACACATA	50849
rs32138397	snp	A/C			intron-variant, upstream-variant-2KB	Rnf10	Mm_Celera	5:115260782	CAGAGTTAACACATA[A/C]ACGCTGAGCTCCAGG	50849
rs32138398	snp	A/C			intron-variant, upstream-variant-2KB	Rnf10	Mm_Celera	5:115261929	TCTAATTTCACATAA[A/C]AGTACTGAAGATTAT	50849
rs32138399	snp	C/T			intron-variant	Rnf10	Mm_Celera	5:115262259	TATCTGTTGACCAAA[C/T]ATCTATACTCTGGGT	50849
rs32138400	snp	A/G			intron-variant	Rnf10	Mm_Celera	5:115262644	CAGCATGACTAATGA[A/G]CTTTAACAAGGAACA	50849
rs32138401	snp	A/C			intron-variant	Rnf10	Mm_Celera	5:115263090	CGGAGGTGTTAGTGG[A/C]GGCTGCAGCTGGTAC	50849
rs32138402	snp	C/G			intron-variant	Rnf10	Mm_Celera	5:115263476	CTTTTGTATGATAGC[C/G]ATCCTGTTTCAACTT	50849
rs32138403	snp	A/G			intron-variant	Rnf10	Mm_Celera	5:115263531	TGTCTGACATGAACC[A/G]TGAATGATCTTGTCA	50849
rs32138543	snp	C/T			intron-variant	Rnf10	Mm_Celera	5:115243658	TCACAGGGTAACCTA[C/T]TCTGGTTGAAGTTCT	50849
rs32139034	snp	A/G			intron-variant	Rnf10	GRCm38.p3	5:115265670	TTTTCATGTGTGGAA[A/G]TTTTCGTGTGTATAC	50849
rs32139214	snp	A/G			intron-variant	Rnf10	Mm_Celera	5:115243874	CTCTGTCCTGAGCCA[A/G]TCTCTCAGCACTGTG	50849
rs32139215	snp	A/G			intron-variant	Rnf10	Mm_Celera	5:115243899	ACTGTGCATGTGGTG[A/G]TGATGTGGGTGATGC	50849
rs32139216	snp	A/G			intron-variant	Rnf10	Mm_Celera	5:115244013	GCTTTCTCAAGCAAA[A/G]GATTTACCTGGGCAA	50849
rs32139217	snp	C/G/T			intron-variant	Rnf10	GRCm38.p3	5:115244175	TTTAATGAGAAACAA[C/G/T]CATGAGAGCCAGGCA	50849
rs32139218	snp	C/T			intron-variant	Rnf10	GRCm38.p3	5:115244378	TTAATCCTGCCCTGT[C/T]CTTATTCCAGAGTAC	50849
rs32139219	snp	C/T			intron-variant	Rnf10	GRCm38.p3	5:115244391	GTTCTTATTCCAGAG[C/T]ACTAGGCATTGCCTA	50849
rs32139220	snp	A/G			intron-variant	Rnf10	GRCm38.p3	5:115244418	CCTACACCAGTGAAC[A/G]CAGACAAGAGGCTTC	50849
rs32139221	snp	C/T			intron-variant	Rnf10	GRCm38.p3	5:115244452	AAGCTCCTTTAACAC[C/T]GGCATGCAACCACAG	50849
rs32139222	snp	A/G			intron-variant	Rnf10	GRCm38.p3	5:115244590	AAATAAAAACAGAAA[A/G]GCTTGCTAGCTCTCC	50849
rs32139223	snp	A/G			intron-variant	Rnf10	GRCm38.p3	5:115244599	CAGAAAGGCTTGCTA[A/G]CTCTCCAAGCTGAGA	50849
rs32139804	snp	A/G			intron-variant	Rnf10	GRCm38.p3	5:115244658	TGGACAACTTCAGAA[A/G]AAACATCCAGATCAC	50849
rs32139805	snp	A/G			intron-variant	Rnf10	Mm_Celera	5:115244686	CACTGTTGTGGCCAC[A/G]ATGCCCTGGCAGTCA	50849
rs32139806	snp	C/T			intron-variant	Rnf10	Mm_Celera	5:115244830	CTAGGCGGTGGGCAC[C/T]GGGCAGTGGGCACCT	50849
rs32139807	snp	G/T			intron-variant	Rnf10	Mm_Celera	5:115244866	CTCTCTTTCCTAGTA[G/T]CAGGTCCTTCCACAC	50849
rs32139808	snp	G/T			intron-variant	Rnf10	Mm_Celera	5:115245108	CCCCGTTCCTGCCAC[G/T]GAAGTTCCTGTAGAT	50849
rs32139809	snp	C/T			intron-variant	Rnf10	Mm_Celera	5:115245394	TTACAATCAATATTA[C/T]GAAAGGACATTATAA	50849
rs32139810	snp	A/G			intron-variant	Rnf10	Mm_Celera	5:115245401	CAATATTATGAAAGG[A/G]CATTATAAACATTAA	50849
rs32139811	snp	A/G			intron-variant	Rnf10	Mm_Celera	5:115245452	AGAACAGATGGGTCA[A/G]AAAAATGATGCAGGC	50849
rs32139812	snp	C/T			intron-variant	Rnf10	Mm_Celera	5:115245605	TTCAGACACTAGAGT[C/T]TGCTTATGACGGTCA	50849
rs32139813	snp	C/T			intron-variant	Rnf10	Mm_Celera	5:115246029	AAAGGCAATGGAGGT[C/T]CATGTACACAGCTGG	50849
rs32140624	snp	A/C			intron-variant	Rnf10	Mm_Celera	5:115246093	ACTATCAGGCTGTCT[A/C]TGCTTTACAGTAATC	50849
rs32140625	snp	A/G			intron-variant	Rnf10	Mm_Celera	5:115246126	GACAGCAGGAGGCCC[A/G]GGCAGTAAGAGTAGC	50849
rs32140626	snp	C/T			intron-variant	Rnf10	Mm_Celera	5:115246138	CCCAGGCAGTAAGAG[C/T]AGCCTAAGATATGTC	50849
rs32140627	snp	A/G			intron-variant	Rnf10	Mm_Celera	5:115246146	GTAAGAGTAGCCTAA[A/G]ATATGTCAGGATCCT	50849
rs32140628	snp	A/G			intron-variant	Rnf10	Mm_Celera	5:115246210	GTACCTTCACCTCTG[A/G]GGGGTAGGCAGTTCA	50849
rs32140629	snp	A/G			intron-variant	Rnf10	Mm_Celera	5:115246253	CCTAACTGAGCTACT[A/G]TCTCACAAACTTCTC	50849
rs32140630	snp	C/T			intron-variant	Rnf10	Mm_Celera	5:115246368	CAGAGCAAGCTGTGC[C/T]GACCACTCTAATGGA	50849
rs32140631	snp	C/G			intron-variant	Rnf10	Mm_Celera	5:115246486	AGTGGGCATGAGCTC[C/G]CTCTGAGCCTGGAGT	50849
rs32140632	snp	A/G			intron-variant	Rnf10	Mm_Celera	5:115246589	GTCAAATCAGAAACT[A/G]TTCCCAGCTCAGCAG	50849
rs32140633	snp	A/C			intron-variant	Rnf10	Mm_Celera	5:115246763	GAACAGTTCATTATC[A/C]CCTTCACTATCTTAC	50849
rs32141444	snp	A/G			intron-variant	Rnf10	Mm_Celera	5:115246872	GCAACCGTGAGCTCT[A/G]AACTTACACCTGCCC	50849
rs32141445	snp	A/G			missense	Rnf10	Mm_Celera	5:115246931	TGCGCTCTCGGCGAC[A/G]CTCCTCGCGAGCCTT	50849
rs32141446	snp	C/T			intron-variant	Rnf10	Mm_Celera	5:115247010	AAGTTGTAAGAAAGA[C/T]GGATCAGCCACTGTT	50849
rs32141447	snp	A/G			intron-variant	Rnf10	Mm_Celera	5:115247020	AAAGATGGATCAGCC[A/G]CTGTTAACTCTCCCT	50849
rs32141448	snp	G/T			intron-variant	Rnf10	Mm_Celera	5:115247056	ACCACAGCTAAGCCA[G/T]CGAGACAGCAGACCA	50849
rs32141449	snp	C/T			intron-variant	Rnf10	Mm_Celera	5:115247093	TGGGTGCATCCCGTG[C/T]GTGTCTCAGCATACA	50849
rs32141450	snp	A/T			intron-variant	Rnf10	Mm_Celera	5:115247155	AGCAGAGAAGGGCAA[A/T]GGGGCTTTCTCACCT	50849
rs32141451	snp	C/T			intron-variant	Rnf10	Mm_Celera	5:115247366	CCAGAACTAAATGGA[C/T]AGCGCTGCTGCCACT	50849
rs32141452	snp	A/G	0.48	0.0979796	intron-variant	Rnf10	Mm_Celera	5:115247645	GAGGGAATCTGGTCC[A/G]GAACACTGGAAACCA	50849
rs32141453	snp	A/T			intron-variant	Rnf10	Mm_Celera	5:115248209	GACAGGACACCCTGC[A/T]CTGAACCCTAGCACA	50849
rs32142224	snp	A/G			intron-variant	Rnf10	Mm_Celera	5:115248232	CTAGCACAATCAGAG[A/G]GGCATGTGGGGCTAT	50849
rs32142225	snp	A/G			intron-variant	Rnf10	Mm_Celera	5:115248370	GATGAGAGCATCACC[A/G]CAAAAGCCAAGTAAT	50849
rs32142226	snp	A/G	0.375	0.216506	intron-variant	Rnf10	Mm_Celera	5:115248571	TACTTCTTTTCTCCA[A/G]AAAACCTCACCTCAG	50849
rs32142227	snp	A/G			intron-variant	Rnf10	Mm_Celera	5:115248728	CCGCTAAAGACAAGA[A/G]CTCTATCACACAAGC	50849
rs32142228	snp	C/G			synonymous-codon	Rnf10	Mm_Celera	5:115248952	AGAGCTGCTGAGCTG[C/G]GTGAAGCCTGGCTTA	50849
rs32142229	snp	C/G			intron-variant	Rnf10	Mm_Celera	5:115249198	ACCCTAGGTCAACAC[C/G]AAGTCCCATGTTCTG	50849
rs32142230	snp	A/G			intron-variant	Rnf10	Mm_Celera	5:115249296	ACCACCCCTGGAAAA[A/G]GTGACAGATCTAGTC	50849
rs32142231	snp	C/T			intron-variant	Rnf10	Mm_Celera	5:115249330	AGGACACAGCCAAGC[C/T]ACCATCTCTCCTTCA	50849
rs32142232	snp	A/G			intron-variant	Rnf10	Mm_Celera	5:115249377	AGGACAAGTCACTTC[A/G]TTGTGATGGGCACAC	50849

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